Mat-Pilates Exercises on Balance in Adolescents With Scoliosis

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age12-15
SponsorBeni-Suef University

About this trial

The aim of this study is to examine the effects of mat-Pilates exercises on balance and functional capacity in adolescents with scoliosis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adolescents ages will be ranged from 12 to 15 years old.

Cobb's angles ranging from 10° to 25°.

Functional Hearing and vision.

Independent standing and walking.

Disqualifiers

Either spine, upper, or lower limbs fractures.

Leg length discrepancy or foot deformities.

Rheumatic and congenital heart disease.

History of previous surgical operation.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Conventional Physical Therapy

    Other intervention

    It includes stretching exercises of the concave side muscles, strengthening exercises of the convex side muscles, postural control exercises from sitting and standing, and breathing exercises.

  • Mat-Pilates Exercises

    Other intervention

    It includes a selected pilates exercises in the form of bridge, hundred, alternate toe taps, single leg circles, side to side, side kick lying, quadruped, spine twist, side leg raise, and tandem walking

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Conventional Physical TherapyActive comparator 1 intervention
Group B: Mat-PilatesExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Balance

Biodex Stability System will be used to measure overall stability index, anteroposterior stability index and mediolateral stability index.

Time frame
Up to 12 weeks

Secondary outcomes

1

Functional Capacity

Six-minute walk test will be used for measuring functional capacity. It is a sub-maximal test of aerobic capacity, in which the subjects walk as far as possible in 6 minutes (min.) around a premeasured distance.

Time frame
Up to 12 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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